The effect of π-conjugation in the macrocyclic ring on the photophysical properties of a series of thiaaceneporphyrinoids

Young Mo Sung, Bartosz Szyszko, Radomir Myśliborski, Marcin Stȩpień, Juwon Oh, Minjung Son, Lechosław Latos-Grazyński, Dongho Kim

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Abstract

In a series of thiaaceneporphyrinoids, their conformers exhibit macrocyclic π-conjugation pathways controlled by a dihedral angle between the porphyrin framework and acene planes. Conformational equilibria significantly affect the photophysical properties of these macrocycles. This journal is

Original languageEnglish
Pages (from-to)8367-8369
Number of pages3
JournalChemical Communications
Volume50
Issue number61
DOIs
Publication statusPublished - 2014 Aug 7

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All Science Journal Classification (ASJC) codes

  • Catalysis
  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Chemistry(all)
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry

Cite this

Sung, Y. M., Szyszko, B., Myśliborski, R., Stȩpień, M., Oh, J., Son, M., Latos-Grazyński, L., & Kim, D. (2014). The effect of π-conjugation in the macrocyclic ring on the photophysical properties of a series of thiaaceneporphyrinoids. Chemical Communications, 50(61), 8367-8369. https://doi.org/10.1039/c4cc03855j